3ou3

MDR769 HIV-1 protease complexed with PR/RT hepta-peptide

Method: X-RAY DIFFRACTION Dmax: 62.2 Å Quality: REASONABLE

1. Protein Identity and Related Structures Protein Identity & Related Structures

HIV-1 protease

Human immunodeficiency virus 1

UniProt Q000H7

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–99 Chain B; UniProt 1–99 Not recorded PR/RT substrate peptide × 1 (Q9YV20) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.8;298 K;0.8M NaCl 01 M MES , pH 5.8, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.70 Å R-free 0.226

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

20 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q000H7_9HIV1
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–99; UniProt 1–99 Author chain B; PDBConstruct 1–99; UniProt 1–99

PR/RT substrate peptide

OrganismNot specified

UniProt Q9YV20

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 153–159 Not recorded HIV-1 protease × 2 (Q000H7) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.8;298 K;0.8M NaCl 01 M MES , pH 5.8, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.70 Å R-free 0.226

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q9YV20_9HIV1
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–7; UniProt 153–159

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 3ou3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3ou3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3ou3
Deposition date deposition_date2010-09-14
Structure title titleMDR769 HIV-1 protease complexed with PR/RT hepta-peptide
Keywords keywords;MDR HIV-1 protease, inhibitor, drug resistance, substrate envelope, HIV-1 protease, protease, PR/RT substrate peptide, none, HYDROLASE, HYDROLASE-PEPTIDE complex ;; HYDROLASE/PEPTIDE
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier18.51
Radius of gyration Rg (electron density) rg_electron17.63
Forward intensity I(0) i08287780.00
Molecular weight molecular_weight22380.0 kDa
Excluded volume excluded_volume28652 ų
Envelope volume envelope_volume33327 ų
Hydration-shell volume shell_volume16210 ų
Envelope diameter envelope_diameter62.6
Shell Rg shell_rg23.26
Envelope Rg envelope_rg17.92
Shape Rg shape_rg17.65
Total Rg total_rg18.55
Total atoms total_atoms1568
Residues n_residues204
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax62.2
Rg (real space) rg_real18.49
Rg uncertainty (real space) rg_real_error0.42
I(0) (real space) i0_real8.2880e+06
I(0) uncertainty (real space) i0_real_error1.0420e+05
Rg (reciprocal space) rg_reciprocal18.50
I(0) (reciprocal space) i0_reciprocal8288000.0000
Solution quality estimate total_estimate0.6521
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.5
Skewness Skewness skewness0.366
Kurtosis Kurtosis kurtosis-0.236
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4082000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.769; Stabil: 1.000; Sysdev: 0.391; Positv: 1.000; Valcen: 0.992; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id3ou3A00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology70 — Cathepsin D, subunit A; domain 1
Homologous superfamily homologous superfamily10 — Acid Proteases
Domain ID domain_id3ou3B00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology70 — Cathepsin D, subunit A; domain 1
Homologous superfamily homologous superfamily10 — Acid Proteases

8. Citations (1)

9. Files and Curves (10)